Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 2 |
Forrest at al. (procyclic) | no | yes: 2 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 5 |
NetGPI | no | yes: 0, no: 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0031201 | SNARE complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0098796 | membrane protein complex | 2 | 1 |
Related structures:
AlphaFold database: E9AJJ4
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 6 |
GO:0006886 | intracellular protein transport | 4 | 6 |
GO:0008104 | protein localization | 4 | 6 |
GO:0009987 | cellular process | 1 | 6 |
GO:0015031 | protein transport | 4 | 6 |
GO:0033036 | macromolecule localization | 2 | 6 |
GO:0045184 | establishment of protein localization | 3 | 6 |
GO:0046907 | intracellular transport | 3 | 6 |
GO:0051179 | localization | 1 | 6 |
GO:0051234 | establishment of localization | 2 | 6 |
GO:0051641 | cellular localization | 2 | 6 |
GO:0051649 | establishment of localization in cell | 3 | 6 |
GO:0070727 | cellular macromolecule localization | 3 | 6 |
GO:0071702 | organic substance transport | 4 | 6 |
GO:0071705 | nitrogen compound transport | 4 | 6 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022411 | cellular component disassembly | 4 | 1 |
GO:0032984 | protein-containing complex disassembly | 5 | 1 |
GO:0035494 | SNARE complex disassembly | 6 | 1 |
GO:0043933 | protein-containing complex organization | 4 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000149 | SNARE binding | 3 | 1 |
GO:0005483 | soluble NSF attachment protein activity | 3 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0005515 | protein binding | 2 | 1 |
GO:0019905 | syntaxin binding | 4 | 1 |
GO:0030674 | protein-macromolecule adaptor activity | 2 | 1 |
GO:0060090 | molecular adaptor activity | 1 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 110 | 114 | PF00656 | 0.536 |
CLV_C14_Caspase3-7 | 310 | 314 | PF00656 | 0.368 |
CLV_C14_Caspase3-7 | 468 | 472 | PF00656 | 0.599 |
CLV_C14_Caspase3-7 | 497 | 501 | PF00656 | 0.502 |
CLV_NRD_NRD_1 | 270 | 272 | PF00675 | 0.368 |
CLV_NRD_NRD_1 | 417 | 419 | PF00675 | 0.558 |
CLV_NRD_NRD_1 | 426 | 428 | PF00675 | 0.500 |
CLV_NRD_NRD_1 | 658 | 660 | PF00675 | 0.579 |
CLV_PCSK_KEX2_1 | 270 | 272 | PF00082 | 0.368 |
CLV_PCSK_KEX2_1 | 417 | 419 | PF00082 | 0.551 |
CLV_PCSK_KEX2_1 | 426 | 428 | PF00082 | 0.488 |
CLV_PCSK_KEX2_1 | 65 | 67 | PF00082 | 0.589 |
CLV_PCSK_KEX2_1 | 658 | 660 | PF00082 | 0.579 |
CLV_PCSK_KEX2_1 | 90 | 92 | PF00082 | 0.707 |
CLV_PCSK_PC1ET2_1 | 65 | 67 | PF00082 | 0.559 |
CLV_PCSK_PC1ET2_1 | 90 | 92 | PF00082 | 0.662 |
CLV_PCSK_SKI1_1 | 295 | 299 | PF00082 | 0.420 |
CLV_PCSK_SKI1_1 | 316 | 320 | PF00082 | 0.420 |
CLV_PCSK_SKI1_1 | 399 | 403 | PF00082 | 0.420 |
CLV_PCSK_SKI1_1 | 427 | 431 | PF00082 | 0.394 |
CLV_PCSK_SKI1_1 | 538 | 542 | PF00082 | 0.454 |
CLV_PCSK_SKI1_1 | 595 | 599 | PF00082 | 0.491 |
CLV_PCSK_SKI1_1 | 617 | 621 | PF00082 | 0.475 |
CLV_PCSK_SKI1_1 | 659 | 663 | PF00082 | 0.576 |
DEG_APCC_DBOX_1 | 502 | 510 | PF00400 | 0.458 |
DEG_APCC_KENBOX_2 | 610 | 614 | PF00400 | 0.491 |
DEG_SPOP_SBC_1 | 465 | 469 | PF00917 | 0.518 |
DOC_CYCLIN_RxL_1 | 313 | 322 | PF00134 | 0.420 |
DOC_CYCLIN_RxL_1 | 532 | 544 | PF00134 | 0.472 |
DOC_CYCLIN_RxL_1 | 656 | 666 | PF00134 | 0.579 |
DOC_MAPK_gen_1 | 503 | 510 | PF00069 | 0.459 |
DOC_MAPK_gen_1 | 90 | 98 | PF00069 | 0.518 |
DOC_MAPK_MEF2A_6 | 346 | 354 | PF00069 | 0.420 |
DOC_MAPK_MEF2A_6 | 503 | 511 | PF00069 | 0.458 |
DOC_MAPK_MEF2A_6 | 91 | 100 | PF00069 | 0.514 |
DOC_PP1_RVXF_1 | 293 | 300 | PF00149 | 0.420 |
DOC_PP2B_LxvP_1 | 238 | 241 | PF13499 | 0.489 |
DOC_PP2B_PxIxI_1 | 349 | 355 | PF00149 | 0.420 |
DOC_USP7_MATH_1 | 120 | 124 | PF00917 | 0.667 |
DOC_USP7_MATH_1 | 138 | 142 | PF00917 | 0.509 |
DOC_USP7_MATH_1 | 200 | 204 | PF00917 | 0.716 |
DOC_USP7_MATH_1 | 300 | 304 | PF00917 | 0.368 |
DOC_USP7_MATH_1 | 353 | 357 | PF00917 | 0.425 |
DOC_USP7_MATH_1 | 445 | 449 | PF00917 | 0.753 |
DOC_USP7_MATH_1 | 465 | 469 | PF00917 | 0.557 |
DOC_USP7_MATH_1 | 559 | 563 | PF00917 | 0.504 |
DOC_USP7_MATH_1 | 77 | 81 | PF00917 | 0.743 |
DOC_WW_Pin1_4 | 226 | 231 | PF00397 | 0.762 |
DOC_WW_Pin1_4 | 244 | 249 | PF00397 | 0.506 |
DOC_WW_Pin1_4 | 253 | 258 | PF00397 | 0.628 |
DOC_WW_Pin1_4 | 436 | 441 | PF00397 | 0.648 |
DOC_WW_Pin1_4 | 572 | 577 | PF00397 | 0.574 |
LIG_14-3-3_CanoR_1 | 194 | 198 | PF00244 | 0.615 |
LIG_14-3-3_CanoR_1 | 250 | 258 | PF00244 | 0.592 |
LIG_14-3-3_CanoR_1 | 270 | 274 | PF00244 | 0.417 |
LIG_14-3-3_CanoR_1 | 489 | 495 | PF00244 | 0.541 |
LIG_14-3-3_CanoR_1 | 624 | 629 | PF00244 | 0.552 |
LIG_Actin_WH2_2 | 331 | 348 | PF00022 | 0.420 |
LIG_APCC_ABBA_1 | 402 | 407 | PF00400 | 0.420 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.672 |
LIG_BIR_III_2 | 47 | 51 | PF00653 | 0.615 |
LIG_BIR_III_4 | 232 | 236 | PF00653 | 0.642 |
LIG_BRCT_BRCA1_1 | 197 | 201 | PF00533 | 0.656 |
LIG_BRCT_BRCA1_1 | 476 | 480 | PF00533 | 0.701 |
LIG_deltaCOP1_diTrp_1 | 289 | 298 | PF00928 | 0.420 |
LIG_FHA_1 | 150 | 156 | PF00498 | 0.635 |
LIG_FHA_1 | 205 | 211 | PF00498 | 0.690 |
LIG_FHA_1 | 292 | 298 | PF00498 | 0.420 |
LIG_FHA_1 | 426 | 432 | PF00498 | 0.530 |
LIG_FHA_1 | 436 | 442 | PF00498 | 0.544 |
LIG_FHA_1 | 465 | 471 | PF00498 | 0.623 |
LIG_FHA_1 | 542 | 548 | PF00498 | 0.405 |
LIG_FHA_2 | 204 | 210 | PF00498 | 0.660 |
LIG_FHA_2 | 627 | 633 | PF00498 | 0.419 |
LIG_FHA_2 | 635 | 641 | PF00498 | 0.377 |
LIG_FHA_2 | 68 | 74 | PF00498 | 0.544 |
LIG_LIR_Gen_1 | 303 | 312 | PF02991 | 0.368 |
LIG_LIR_Gen_1 | 584 | 591 | PF02991 | 0.477 |
LIG_LIR_Gen_1 | 97 | 105 | PF02991 | 0.513 |
LIG_LIR_Nem_3 | 198 | 204 | PF02991 | 0.709 |
LIG_LIR_Nem_3 | 303 | 308 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 584 | 590 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 594 | 600 | PF02991 | 0.413 |
LIG_LIR_Nem_3 | 637 | 641 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 97 | 103 | PF02991 | 0.511 |
LIG_NRBOX | 505 | 511 | PF00104 | 0.454 |
LIG_PCNA_yPIPBox_3 | 23 | 34 | PF02747 | 0.593 |
LIG_PCNA_yPIPBox_3 | 609 | 620 | PF02747 | 0.433 |
LIG_PTAP_UEV_1 | 456 | 461 | PF05743 | 0.656 |
LIG_PTB_Apo_2 | 322 | 329 | PF02174 | 0.420 |
LIG_SH2_CRK | 542 | 546 | PF00017 | 0.437 |
LIG_SH2_SRC | 516 | 519 | PF00017 | 0.483 |
LIG_SH2_STAT3 | 364 | 367 | PF00017 | 0.368 |
LIG_SH2_STAT5 | 539 | 542 | PF00017 | 0.487 |
LIG_SH2_STAT5 | 586 | 589 | PF00017 | 0.493 |
LIG_SH2_STAT5 | 596 | 599 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 641 | 644 | PF00017 | 0.332 |
LIG_SH3_3 | 13 | 19 | PF00018 | 0.685 |
LIG_SH3_3 | 454 | 460 | PF00018 | 0.524 |
LIG_SH3_3 | 475 | 481 | PF00018 | 0.635 |
LIG_SH3_3 | 93 | 99 | PF00018 | 0.507 |
LIG_SUMO_SIM_par_1 | 236 | 242 | PF11976 | 0.568 |
LIG_TRAF2_1 | 275 | 278 | PF00917 | 0.368 |
LIG_TRAF2_1 | 390 | 393 | PF00917 | 0.368 |
LIG_TYR_ITIM | 540 | 545 | PF00017 | 0.438 |
LIG_UBA3_1 | 383 | 391 | PF00899 | 0.368 |
LIG_WW_1 | 485 | 488 | PF00397 | 0.641 |
MOD_CDK_SPxK_1 | 244 | 250 | PF00069 | 0.478 |
MOD_CK1_1 | 171 | 177 | PF00069 | 0.600 |
MOD_CK1_1 | 195 | 201 | PF00069 | 0.636 |
MOD_CK1_1 | 203 | 209 | PF00069 | 0.711 |
MOD_CK1_1 | 256 | 262 | PF00069 | 0.381 |
MOD_CK1_1 | 558 | 564 | PF00069 | 0.579 |
MOD_CK1_1 | 76 | 82 | PF00069 | 0.737 |
MOD_CK2_1 | 203 | 209 | PF00069 | 0.690 |
MOD_CK2_1 | 634 | 640 | PF00069 | 0.401 |
MOD_CK2_1 | 67 | 73 | PF00069 | 0.545 |
MOD_GlcNHglycan | 108 | 112 | PF01048 | 0.572 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.676 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.554 |
MOD_GlcNHglycan | 175 | 178 | PF01048 | 0.707 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.609 |
MOD_GlcNHglycan | 197 | 200 | PF01048 | 0.648 |
MOD_GlcNHglycan | 221 | 224 | PF01048 | 0.708 |
MOD_GlcNHglycan | 232 | 236 | PF01048 | 0.613 |
MOD_GlcNHglycan | 241 | 244 | PF01048 | 0.519 |
MOD_GlcNHglycan | 258 | 261 | PF01048 | 0.378 |
MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.744 |
MOD_GlcNHglycan | 443 | 446 | PF01048 | 0.681 |
MOD_GlcNHglycan | 52 | 56 | PF01048 | 0.673 |
MOD_GlcNHglycan | 557 | 560 | PF01048 | 0.521 |
MOD_GlcNHglycan | 561 | 564 | PF01048 | 0.528 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.617 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.761 |
MOD_GlcNHglycan | 86 | 89 | PF01048 | 0.643 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.697 |
MOD_GSK3_1 | 116 | 123 | PF00069 | 0.691 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.637 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.726 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.607 |
MOD_GSK3_1 | 334 | 341 | PF00069 | 0.420 |
MOD_GSK3_1 | 441 | 448 | PF00069 | 0.658 |
MOD_GSK3_1 | 490 | 497 | PF00069 | 0.565 |
MOD_GSK3_1 | 555 | 562 | PF00069 | 0.602 |
MOD_GSK3_1 | 572 | 579 | PF00069 | 0.534 |
MOD_GSK3_1 | 586 | 593 | PF00069 | 0.320 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.734 |
MOD_LATS_1 | 487 | 493 | PF00433 | 0.420 |
MOD_N-GLC_1 | 329 | 334 | PF02516 | 0.368 |
MOD_NEK2_1 | 129 | 134 | PF00069 | 0.620 |
MOD_NEK2_1 | 149 | 154 | PF00069 | 0.626 |
MOD_NEK2_1 | 319 | 324 | PF00069 | 0.420 |
MOD_NEK2_1 | 345 | 350 | PF00069 | 0.420 |
MOD_NEK2_1 | 425 | 430 | PF00069 | 0.456 |
MOD_NEK2_1 | 498 | 503 | PF00069 | 0.428 |
MOD_NEK2_1 | 541 | 546 | PF00069 | 0.446 |
MOD_NEK2_2 | 300 | 305 | PF00069 | 0.368 |
MOD_NEK2_2 | 581 | 586 | PF00069 | 0.522 |
MOD_PIKK_1 | 6 | 12 | PF00454 | 0.701 |
MOD_PIKK_1 | 77 | 83 | PF00454 | 0.554 |
MOD_PK_1 | 474 | 480 | PF00069 | 0.585 |
MOD_PKA_1 | 555 | 561 | PF00069 | 0.542 |
MOD_PKA_2 | 129 | 135 | PF00069 | 0.615 |
MOD_PKA_2 | 149 | 155 | PF00069 | 0.523 |
MOD_PKA_2 | 193 | 199 | PF00069 | 0.737 |
MOD_PKA_2 | 249 | 255 | PF00069 | 0.614 |
MOD_PKA_2 | 269 | 275 | PF00069 | 0.225 |
MOD_PKA_2 | 425 | 431 | PF00069 | 0.394 |
MOD_PKA_2 | 488 | 494 | PF00069 | 0.600 |
MOD_Plk_1 | 169 | 175 | PF00069 | 0.504 |
MOD_Plk_1 | 192 | 198 | PF00069 | 0.519 |
MOD_Plk_1 | 603 | 609 | PF00069 | 0.541 |
MOD_Plk_4 | 300 | 306 | PF00069 | 0.407 |
MOD_Plk_4 | 319 | 325 | PF00069 | 0.260 |
MOD_Plk_4 | 353 | 359 | PF00069 | 0.372 |
MOD_Plk_4 | 581 | 587 | PF00069 | 0.520 |
MOD_ProDKin_1 | 226 | 232 | PF00069 | 0.762 |
MOD_ProDKin_1 | 244 | 250 | PF00069 | 0.508 |
MOD_ProDKin_1 | 253 | 259 | PF00069 | 0.616 |
MOD_ProDKin_1 | 436 | 442 | PF00069 | 0.647 |
MOD_ProDKin_1 | 572 | 578 | PF00069 | 0.569 |
MOD_SUMO_for_1 | 390 | 393 | PF00179 | 0.368 |
TRG_DiLeu_BaEn_1 | 261 | 266 | PF01217 | 0.420 |
TRG_ENDOCYTIC_2 | 542 | 545 | PF00928 | 0.474 |
TRG_ER_diArg_1 | 292 | 295 | PF00400 | 0.225 |
TRG_ER_diArg_1 | 417 | 419 | PF00400 | 0.548 |
TRG_ER_diArg_1 | 425 | 427 | PF00400 | 0.503 |
TRG_Pf-PMV_PEXEL_1 | 496 | 500 | PF00026 | 0.540 |
TRG_Pf-PMV_PEXEL_1 | 659 | 663 | PF00026 | 0.571 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S5H4Z6 | Leishmania donovani | 76% | 97% |
A4H3C9 | Leishmania braziliensis | 56% | 100% |
A4HRM8 | Leishmania infantum | 76% | 97% |
E9ACA6 | Leishmania major | 75% | 99% |